Canonical Allele Identifier: CA2495876129

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480829_47480832delinsTATC , CM000664.2:g.47480829_47480832delinsTATC	GRCh38
NC_000002.11:g.47707968_47707971delinsTATC , CM000664.1:g.47707968_47707971delinsTATC	GRCh37
NC_000002.10:g.47561472_47561475delinsTATC	NCBI36
NG_007110.2:g.82706_82709delinsTATC , LRG_218:g.82706_82709delinsTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2592_2595delinsTATC	ENSP00000495641.2:p.Asp864=
ENST00000233146.7:c.2592_2595delinsTATC MANE Select	ENSP00000233146.2:p.Asp864=
ENST00000543555.6:c.2394_2397delinsTATC	ENSP00000442697.1:p.Asp798=
ENST00000644092.1:c.*892_*895delinsTATC	ENSP00000496351.1:n.*892_*895delinsTATC
ENST00000644900.1:c.445_448delinsTATC
ENST00000645339.1:c.2592_2595delinsTATC	ENSP00000496441.1:p.Asp864=
ENST00000645506.1:c.2592_2595delinsTATC	ENSP00000495455.1:p.Asp864=
ENST00000646415.1:c.2592_2595delinsTATC	ENSP00000495543.1:p.Asp864=
ENST00000233146.6:c.2592_2595delinsTATC	ENSP00000233146.2:p.Asp864=
ENST00000406134.5:c.2592_2595delinsTATC	ENSP00000384199.1:p.Asp864=
ENST00000461394.5:n.33_36delinsTATC
ENST00000543555.5:c.2394_2397delinsTATC	ENSP00000442697.1:p.Asp798=
ENST00000610696.4:c.*988_*991delinsTATC	ENSP00000483159.1:n.*988_*991delinsTATC
ENST00000613514.4:c.*1132_*1135delinsTATC	ENSP00000484137.1:n.*1132_*1135delinsTATC
ENST00000617333.3:c.*1358_*1361delinsTATC	ENSP00000482468.1:n.*1358_*1361delinsTATC
ENST00000617938.4:c.*1564_*1567delinsTATC	ENSP00000481158.1:n.*1564_*1567delinsTATC
ENST00000621359.2:c.*158_*161delinsTATC	ENSP00000481416.1:n.*158_*161delinsTATC
NM_000251.2:c.2592_2595delinsTATC , LRG_218t1:c.2592_2595delinsTATC	NP_000242.1:p.Asp864=
NM_001258281.1:c.2394_2397delinsTATC	NP_001245210.1:p.Asp798=
XM_005264332.2:c.2592_2595delinsTATC	XP_005264389.2:p.Asp864=
XM_011532867.1:c.2592_2595delinsTATC	XP_011531169.1:p.Asp864=
XR_939685.1:n.2664_2667delinsTATC
XM_005264332.4:c.2592_2595delinsTATC	XP_005264389.2:p.Asp864=
XM_011532867.2:c.2592_2595delinsTATC	XP_011531169.1:p.Asp864=
XR_001738747.2:n.2654_2657delinsTATC
XR_939685.2:n.2654_2657delinsTATC
NM_000251.3:c.2592_2595delinsTATC MANE Select	NP_000242.1:p.Asp864=